Variant report

Variant	rs61863305
Chromosome Location	chr10:99458957-99458958
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12218718	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4561136	0.82[EUR][1000 genomes]
rs7896659	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7905308	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7908350	0.83[ASN][1000 genomes]
rs7922721	0.83[ASN][1000 genomes]
rs9787703	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1817777	chr10:99196035-99558169	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:99452200-99459400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr10:99458200-99460600	Weak transcription	Hela-S3	cervix
3	chr10:99458200-99460600	Weak transcription	HepG2	liver
4	chr10:99458200-99461000	Weak transcription	NHDF-Ad	bronchial
5	chr10:99458400-99459400	Weak transcription	Fetal Intestine Small	intestine
6	chr10:99458400-99461200	Weak transcription	Stomach Mucosa	stomach
7	chr10:99458600-99459600	Enhancers	GM12878-XiMat	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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